The nuclear cleavage of a suboptimal primary miRNA hairpin by the Drosha/DGCR8 complex ("Microprocessor") can be enhanced by an optimal miRNA neighbor, a phenomenon termed cluster assistance. Several features and biological impacts of this new layer of miRNA regulation are not fully known. Here, we elucidate the parameters of cluster assistance of a suboptimal miRNA and also reveal competitive interactions amongst optimal miRNAs within a cluster. We exploit cluster assistance as a functional assay for suboptimal processing and use this to invalidate putative suboptimal substrates, as well as identify a "solo" suboptimal miRNA. Finally, we report complexity in how specific mutations might affect the biogenesis of clustered miRNAs in disease contexts. This includes how an operon context can buffer the effect of a deleterious processing var-iant, but reciprocally how a point mutation can have a nonautonomous effect to impair the biogenesis of a clustered, suboptimal, neighbor. These data expand our knowledge regarding regulated miRNA biogenesis in humans and represent a functional assay for empirical definition of suboptimal Microprocessor substrates.
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Seoul Natl Univ, Dept Appl Biol & Chem, Seoul 08826, South KoreaSeoul Natl Univ, Dept Appl Biol & Chem, Seoul 08826, South Korea
Park, Sehee
Kang, Igojo
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Seoul Natl Univ, Dept Agr Biotechnol, Seoul 08826, South KoreaSeoul Natl Univ, Dept Appl Biol & Chem, Seoul 08826, South Korea
Kang, Igojo
Shin, Chanseok
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Seoul Natl Univ, Dept Agr Biotechnol, Seoul 08826, South Korea
Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 08826, South Korea
Seoul Natl Univ, Plant Genom & Breeding Inst, Seoul 08826, South Korea
Seoul Natl Univ, Res Ctr Plant Plast, Seoul 08826, South KoreaSeoul Natl Univ, Dept Appl Biol & Chem, Seoul 08826, South Korea